Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP772891.RACJph_lGAw_Ip-dDIYtdzcCLTdaCxY1AmqDjgi7ScOgI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP772891.RACJph_lGAw_Ip-dDIYtdzcCLTdaCxY1AmqDjgi7ScOgI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP772891.RACJph_lGAw_Ip-dDIYtdzcCLTdaCxY1AmqDjgi7ScOgI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP772891.RACJph_lGAw_Ip-dDIYtdzcCLTdaCxY1AmqDjgi7ScOgI130_provenance.
- befree-2016 importedOn "2016-02-19" NP772891.RACJph_lGAw_Ip-dDIYtdzcCLTdaCxY1AmqDjgi7ScOgI130_provenance.
- NP772891.RACJph_lGAw_Ip-dDIYtdzcCLTdaCxY1AmqDjgi7ScOgI130_assertion wasGeneratedBy ECO_0000203 NP772891.RACJph_lGAw_Ip-dDIYtdzcCLTdaCxY1AmqDjgi7ScOgI130_provenance.
- NP772891.RACJph_lGAw_Ip-dDIYtdzcCLTdaCxY1AmqDjgi7ScOgI130_assertion wasDerivedFrom befree-2016 NP772891.RACJph_lGAw_Ip-dDIYtdzcCLTdaCxY1AmqDjgi7ScOgI130_provenance.
- NP772891.RACJph_lGAw_Ip-dDIYtdzcCLTdaCxY1AmqDjgi7ScOgI130_assertion SIO_000772 19878917 NP772891.RACJph_lGAw_Ip-dDIYtdzcCLTdaCxY1AmqDjgi7ScOgI130_provenance.
- NP772891.RACJph_lGAw_Ip-dDIYtdzcCLTdaCxY1AmqDjgi7ScOgI130_assertion evidence source_evidence_literature NP772891.RACJph_lGAw_Ip-dDIYtdzcCLTdaCxY1AmqDjgi7ScOgI130_provenance.
- NP772891.RACJph_lGAw_Ip-dDIYtdzcCLTdaCxY1AmqDjgi7ScOgI130_assertion description "[Recessive mutations of the gene TRPM1 abrogate ON bipolar cell function and cause complete congenital stationary night blindness in humans.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP772891.RACJph_lGAw_Ip-dDIYtdzcCLTdaCxY1AmqDjgi7ScOgI130_provenance.